3496-81-9

Basic information

• Product Name: 1-cyclohexyl-3-propan-2-ylurea
• CAS NO: 3496-81-9
• Molecular Formula: C₁₀H₂₀N₂O
• Molecular Weight: 184.2786
• Mol File: 3496-81-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 342°C at 760 mmHg
• Flash Point: 139.6°C
• Density: 0.97g/cm³
• Vapor Pressure: 7.77E-05mmHg at 25°C
• Refractive Index: 1.479
• CAS DataBase Reference: 1-cyclohexyl-3-propan-2-ylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-cyclohexyl-3-propan-2-ylurea(3496-81-9)
• EPA Substance Registry System: 1-cyclohexyl-3-propan-2-ylurea(3496-81-9)

Safety Data

• Hazardous Substances Data: 3496-81-9(Hazardous Substances Data)

Usage

Structure

Urea derivative with a cyclohexyl group and an isopropyl group attached to the nitrogen atom

Usage

Organic intermediate in the synthesis of pharmaceuticals and agrochemicals, corrosion inhibitor in water treatment processes, stabilizer in the production of plastics and rubber

Potential

Studied for its potential as an antitumor agent

Upstream product

• 1122-56-1 cyclohexylcarboxamide 
• 75-31-0 isopropylamine 
• 563-83-7 ISOPROPYLAMIDE 
• 108-91-8 cyclohexylamine 
• 92109-08-5 cyclohexylcarbamic acid 4-nitrophenyl ester 
• 34780-31-9 N-cyclohexyl-N'-isopropylthiourea 

Downstream Products

• 3385-48-6 N¹-Isopropyl-N²-cyclohexyl-formamidin 
• 3496-83-1 N-cyclohexyl-N'-isopropylcarbodiimide 

Relevant articles and documents

Highly efficient synthesis of ureas and carbamates from amides by iodosylbenzene-induced hofmann rearrangement

A simple and efficient method for the synthesis of 1,3-disubstituted ureas and carbamates from amides by using iodosylbenzene as the oxidant is described. Symmetric and asymmetric ureas and carbamates can be prepared by this procedure in up to 98 % yield. Ureidopeptides can also be prepared in good yield by this method. A simple and efficient method for the synthesis of 1,3-disubstituted ureas and carbamates from amides by using iodosylbenzene as the oxidant is described. By using this method, heterocyclic products can be easily obtained in excellent yield. Ureidopeptides can also be prepared in good yield by this procedure. Copyright